![Boron, difluoro[3-[(2-quinolyl-κN)amino]-1H-isoindol-1-onato-κN2]-, (T-4)-](https://resource.bocsci.com/structure/1519003-31-6.gif?v=2025011501)
Boron, difluoro[3-[(2-quinolyl-κN)amino]-1H-isoindol-1-onato-κN2]-, (T-4)- | 1519003-31-6
Catalog Number | F01-0116 |
Category | BODIPY |
Molecular Formula | C17H10BF2N3O |
Molecular Weight | 321.094 |
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Product Introduction
BODIPY dyes are used to generate fluorescent conjugates of proteins, nucleotides, oligonucleotides and dextrans, as well as to prepare fluorescent enzyme substrates, fatty acids, phospholipids, lipopolysaccharides, receptor ligands and polystyrene microspheres.
- Product Specification
- Application
Excitation | 649 |
Emission | 667 |
Storage | Store at -20°C |
Boron difluoro[3-[(2-quinolyl-κN)amino]-1H-isoindol-1-onato-κN2]- (T-4) is a synthetic compound with potential applications in material science and chemical research.
Luminescent Materials: This boron-based compound can be used in the development of luminescent materials for advanced optical devices. Its distinct electronic properties enable it to emit light when excited, making it valuable for applications in organic light-emitting diodes (OLEDs) and other display technologies. Researchers explore its utility in creating more efficient and durable lighting solutions.
Sensors and Detection: The unique structural features of this compound facilitate its use in chemical sensors. It can be engineered to detect specific ions or molecules, aiding in environmental monitoring and industrial process control. By incorporating it into sensor platforms, scientists can enhance selectivity and sensitivity for various analytical applications.
Catalysis: Boron difluoro compounds are of interest in the field of catalysis due to their ability to facilitate organic transformations. This particular compound can serve as a catalyst in reactions that require the activation of small molecules, such as hydrogenation and hydroboration processes. Its catalytic activity is explored to develop more sustainable and efficient chemical manufacturing methods.
Phosphorescent Probes: The compound's strong phosphorescent properties make it suitable for designing phosphorescent probes for biological imaging. These probes can be utilized in cellular and molecular imaging to study biological processes with high sensitivity and resolution. This aids researchers in visualizing interactions and phenomena within biological systems for clinical and diagnostic purposes.
Applications of Fluorescent Probes & Dyes
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